Evidence map›Paper›PMID 36906534›Full record

ReviewMolecular cancer2023

Extracellular matrix remodeling in tumor progression and immune escape: from mechanisms to treatments.

Zhennan Yuan, Yingpu Li, Sifan Zhang, Xueying Wang, He Dou, Xi Yu, Zhiren Zhang, Shanshan Yang, Min Xiao

Open access · goldFull text readReview
In one paragraph

Review in Molecular cancer, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 616 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
616citing papers in PubMed, 1 pooled it
198.8field-weighted citation impact, top 1% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

616 citing papers in PubMed, 1 synthesis or guideline pooled it, 801 citations in OpenAlex.

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556 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

9 authors at 3 institutions in 1 country.

Zhennan Yuan *Department of Oncological Surgery, Harbin Medical University Cancer Hospital, Harbin, 150081, China.
Yingpu Li *Department of Oncological Surgery, Harbin Medical University Cancer Hospital, Harbin, 150081, China.
Sifan Zhang *Department of Neurobiology, Harbin Medical University, Harbin, 150081, China.
Xueying Wang *Department of Otolaryngology Head and Neck Surgery, Xiangya Hospital, Central South University, Changsha, 410008, China.
He DouDepartment of Oncological Surgery, Harbin Medical University Cancer Hospital, Harbin, 150081, China.
Xi YuDepartment of Gynecological Oncology, Harbin Medical University Cancer Hospital, Harbin, 150081, China.
Zhiren ZhangNHC Key Laboratory of Cell Transplantation, The First Affiliated Hospital of Harbin Medical University, Harbin, 150001, China.
Shanshan YangDepartment of Gynecological Radiotherapy, Harbin Medical University Cancer Hospital, Harbin, 150000, China. yangshanshan@hrbmu.edu.cn.
Min XiaoDepartment of Oncological Surgery, Harbin Medical University Cancer Hospital, Harbin, 150081, China. xiaomin@hrbmu.edu.cn.
Harbin Medical University · CNThird Affiliated Hospital of Harbin Medical University · CNCentral South University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The malignant tumor is a multi-etiological, systemic and complex disease characterized by uncontrolled cell proliferation and distant metastasis. Anticancer treatments including adjuvant therapies and targeted therapies are effective in eliminating cancer cells but in a limited number of patients. Increasing evidence suggests that the extracellular matrix (ECM) plays an important role in tumor development through changes in macromolecule components, degradation enzymes and stiffness. These variations are under the control of cellular components in tumor tissue via the aberrant activation of signaling pathways, the interaction of the ECM components to multiple surface receptors, and mechanical impact. Additionally, the ECM shaped by cancer regulates immune cells which results in an immune suppressive microenvironment and hinders the efficacy of immunotherapies. Thus, the ECM acts as a barrier to protect cancer from treatments and supports tumor progression. Nevertheless, the profound regulatory network of the ECM remodeling hampers the design of individualized antitumor treatment. Here, we elaborate on the composition of the malignant ECM, and discuss the specific mechanisms of the ECM remodeling. Precisely, we highlight the impact of the ECM remodeling on tumor development, including proliferation, anoikis, metastasis, angiogenesis, lymphangiogenesis, and immune escape. Finally, we emphasize ECM "normalization" as a potential strategy for anti-malignant treatment.

Indexed as

Extracellular MatrixNeoplasmsHumansImmunotherapyTumor MicroenvironmentCancer metabolismCollagen orientationExtracellular matrixImmune escapeImmunotherapyStiffness

Identifiers

PMID36906534
PMCPMC10007858
OpenAlexW4323971780

What OpenQuestion holds

Textfull text, public
LicenceCC BY
measurements read5
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.